Dynamin 1-Like 抗体 (AA 618-736)
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Quick Overview for Dynamin 1-Like 抗体 (AA 618-736) (ABIN7876143)
抗原
See all Dynamin 1-Like (DNM1L) 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 618-736
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原理
- DNM1L Antibody / DRP1
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纯化方法
- Affinity purified
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免疫原
- Recombinant human protein (amino acids Q618-W736) was used as the immunogen for the DNM1L antibody.
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亚型
- IgG
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anti-Dynamin 1-Like (DNM1L) (AA 69-213) antibody
DNM1L 适用: 人 WB, ELISA, IHC 宿主: 小鼠 Monoclonal 4E11B11 unconjugated
anti-Dynamin 1-Like (DNM1L) (AA 69-213) antibodyDNM1L 适用: 人, 小鼠, 大鼠 WB, ELISA, ICC, FACS 宿主: 小鼠 Monoclonal 4A4C7 unconjugated
anti-Dynamin 1-Like (DNM1L) (AA 1-710) antibodyDNM1L 适用: 人 WB, ELISA, IHC (p) 宿主: 小鼠 Monoclonal 3B5 unconjugated
anti-Dynamin 1-Like (DNM1L) antibodyDNM1L 适用: 人, 小鼠, 大鼠, 猴, 犬 WB, IHC, IHC (p) 宿主: 小鼠 Monoclonal 4F6 unconjugated
anti-Dynamin 1-Like (DNM1L) antibodyDNM1L 适用: 人, 小鼠, 大鼠, 猴 WB, IHC, IHC (p) 宿主: 小鼠 Monoclonal 2E7 unconjugated
anti-Dynamin 1-Like (DNM1L) antibodyDNM1L 适用: 人 WB, IHC, IF, IHC (p) 宿主: 小鼠 Monoclonal 3F3 unconjugated
anti-Dynamin 1-Like (DNM1L) (AA 411-710) antibodyDNM1L 适用: 人 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Dynamin 1-Like (DNM1L) antibodyDNM1L 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Dynamin 1-Like (DNM1L) antibodyKD Validated DNM1L 适用: 人 WB, FACS 宿主: 小鼠 Monoclonal 24GB8215 unconjugated
anti-Dynamin 1-Like (DNM1L) (AA 618-736) antibodyDNM1L 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC, IF, ICC, FACS 宿主: 兔 Polyclonal unconjugated
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应用备注
- Optimal dilution of the DNM1L antibody should be determined by the researcher.
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限制
- 仅限研究用
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状态
- Lyophilized
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缓冲液
- 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
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储存条件
- 4 °C,-20 °C
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储存方法
- After reconstitution, the DNM1L antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
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- Dynamin 1-Like (DNM1L)
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别名
- DNM1L
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背景
- Dynamin-1-like protein is a GTPase that regulates mitochondrial fission. In humans, dynamin-1-like protein, which is typically referred to as dynamin-related protein 1 (Drp1), is encoded by the DNM1L gene. The encoded protein mediates mitochondrial and peroxisomal division, and is involved in developmentally regulated apoptosis and programmed necrosis. Dysfunction of this gene is implicated in several neurological disorders, including Alzheimer's disease. Mutations in this gene are associated with the autosomal dominant disorder, encephalopathy, lethal, due to defective mitochondrial and peroxisomal fission (EMPF). Alternative splicing results in multiple transcript variants encoding different isoforms.
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UniProt
- O00429
抗原
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